Canonical Allele Identifier: CA399727831

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42085063A>G (hg19) ; chr17:g.44007695A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007695A>G , CM000679.2:g.44007695A>G	GRCh38
NC_000017.10:g.42085063A>G , CM000679.1:g.42085063A>G	GRCh37
NC_000017.9:g.39440589A>G	NCBI36
NG_008106.1:g.8032A>G
NG_023338.1:g.1775T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1373A>G (NAGS) MANE Select	ENSP00000293404.2:p.Gln458Arg
ENST00000293404.7:c.1373A>G (NAGS)	ENSP00000293404.2:p.Gln458Arg
ENST00000589767.1:c.1304A>G (NAGS)	ENSP00000465408.1:p.Gln435Arg
ENST00000592915.1:n.1261A>G (NAGS)
NM_153006.2:c.1373A>G (NAGS)	NP_694551.1:p.Gln458Arg
XM_011524438.1:c.1268+201A>G (NAGS)	XP_011522740.1:n.1268+201A>G
XM_011524439.1:c.875A>G (NAGS)	XP_011522741.1:p.Gln292Arg
XM_011525035.1:c.-463+15877T>C (PYY)	XP_011523337.1:n.-463+15877T>C
XM_011524439.2:c.875A>G (NAGS)	XP_011522741.1:p.Gln292Arg
NM_153006.3:c.1373A>G (NAGS) MANE Select	NP_694551.1:p.Gln458Arg